Burlington, NC, USA
Job Overview Join LabCorp Diagnostics and you'll be a part of an innovative life sciences company that is deeply integrated in guiding patient care and providing comprehensive clinical laboratory services. With a mission to improve health and improve lives, LabCorp delivers world-class diagnostic solutions and pioneers new diagnostic technologies to improve the delivery of care. As a member of the LabCorp team, you will support a dedicated staff in resulting over 500,000 clinical samples a day, a volume that demands the most accurate and precise analysis possible. You'll join a collegial scientific staff who appreciates that on the other side of every sample, is a person who depends on us! LabCorp is a leader in laboratory medicine and we strive to meet the rapidly evolving healthcare needs. Do work that matters. Join LabCorp and be a part of our team bringing laboratory diagnostics to a new level. Laboratory Corporation of America has immediate openings for Clinical Laboratory Technical Directors nationwide to lead Core and Esoterix testing labs. We are seeking individuals with specialization and experience in one or more of the following areas. Chemistry Toxicology Hematology Flow Cytometry Coagulation Urinalysis Microbiology Molecular Microbiology Endocrinology Therapeutic Drug Monitoring Immunoassay Nucleic Acid Amplification Molecular Genetics NGS Histocompatibility/ HLA testing Education/Qualifications Board Certification in a Clinical specialty PhD in Life Sciences or MD required Experience Depth and breadth of experience within a clinical lab, understanding validation, quality control, proficiency testing, regulatory requirements Minimum of 3-5 years post training experience. Experience in a CLIA/CAP regulated facility highly preferred Direct/Indirect leadership experience Experience interacting and communicating with physicians and clients about questions as it pertains to laboratory tests, results interpretation, etc. Not ready to apply? Connect with us to join our talent community.
Indianapolis, IN, USA
Job Overview We are currently seeking a Senior Director, Medical Affairs - Pathologist to join our team. Reporting to the Vice President, Global Testing Services and Medical Affairs, the incumbent will provide medical consultative and interpretive support to Covance Central Laboratory Services globally and its internal and external customers. The incumbent is responsible for the oversight of medical decision-making and consultation that relate to laboratory services and clinical trials across all sites globally. Additional areas of oversight include consulting with Quality Assurance, Safety Committee, Investigator Site Support, Project Management, Sponsors, and Investigators. The Sr. Med Director will hold the position of team expert and go-to Pathologist and will advise and contribute to final decisions regarding clinical areas of the business. Other areas of responsibilities include; People Leadership: Lead a team of MD Pathologists located both in the US and global Covance sites Laboratory Operations support: Provide medical support and direction to the Laboratory Operations leaders Provide medical/pathology/clinical laboratory support to Laboratory operations departments and Investigators sites as needed. Regulatory and Compliance: As needed or requested, participate in investigator meetings or client visits to provide medical and laboratory support required for the success of a pharmaceutical drug clinical trial and submission of laboratory data to the FDA. Consult with Quality Assurance to ensure compliance with applicable local and international regulations governing clinical reference laboratories, transport of clinical specimens, and pharmaceutical drug clinical trials. Assist in interfacing with Sponsors and/or Regulatory authorities as needed. Scientific support: Assist in the scientific professional growth of laboratory employees (provide guidance for professional development of staff, participates in interviews, makes hiring recommendations, leads disciplinary actions, delivers performance appraisal review, as required) Provide expert input in the creation and approval of reference ranges and appropriate test/method selection for a given clinical indication. Advise in the development and approval of the technical database, the proprietary clinical trials database, and laboratory information systems. Key leader in the review and/or approval of new test or service feasibilities. Contribute to scientific publications. Business development and support: Interact with Sponsors and Medical Affairs group in protocol review and/or development Perform literature review related to the therapeutic area involved in Sponsor clinical development Communicate with clients and clients' Project Managers to promote project schedule adherence within laboratory operations and meet high quality standards. Participate in business development visits to current and potential clients as required. Collaborate with business development in review, writing, presentation and defense proposals Education/Qualifications MD degree, Clinical Pathologist Board Certification Clinical Pathology required Dual Board Certification in Clinical Pathology and Anatomical Pathology preferred Experience Minimum of 10 years experience Strong leadership experience and written/verbal communication skills Laboratory management experience and demonstrated financial awareness Expert knowledge of clinical laboratory systems (testing, operations, finances, and information) Not ready to apply? Connect with us to join our talent community.